Acid gas absorbent composition

ABSTRACT

This invention provides novel compositions comprising substituted polyamines as acid gas scrubbing solutions and methods of using the compositions in an industrial system. The invention relates to the use of such polyamine compounds in industrial processes to remove acidic contaminants from natural and industrial fluid streams, such as natural gas, combustion gas, natural gas, synthesis gas, biogas, and other industrial fluid streams. The compositions and methods of the invention are useful for removal, absorption, or sequestration of acidic contaminants and sulfide contaminants including CO 2 , H 2 S, RSH, CS 2 , COS, and SO.

CROSS REFERENCE TO RELATED APPLICATION

This application is a divisional application of U.S. patent application Ser. No. 12/950,518, “Acid Gas Absorbent Composition, filed on Nov. 19, 2010, currently pending, the disclosure of which is incorporated herein by reference in its entirety.

TECHNICAL FIELD OF THE INVENTION

This invention relates generally to the use of novel compounds as acid gas scrubbing solutions. More specifically, the invention relates to the use of substituted heterocyclic amines and polyamine compounds in industrial processes to remove acidic contaminants from natural and industrial fluid streams, such as natural gas, combustion gas, synthetic gas streams, and hydrocarbon fluids. The invention has particular relevance to processes for removal of carbon dioxide from gas streams having sour gas impurities.

BACKGROUND OF THE INVENTION

Natural gas is a mixture of gaseous hydrocarbons and non-hydrocarbon impurities and contaminants. Removal of, for example, carbon dioxide and acidic sulfide contaminants (e.g., CO₂, H₂S, RSH, CS₂, COS, SO₂, etc.) to meet quality and regulatory requirements in natural gas that is fed into distribution pipelines is a major industrial burden. Such contaminants are often corrosive and may also impair the caloric value of the gas. In addition, increasing concerns of global warming from CO₂ and other emissions has prompted significant investments into methods of capturing such contaminants more efficiently and economically.

Aqueous solutions of commonly available commodity alkanolamines are generally used as scrubbing solutions (chemical absorbents) in gas processing. The purpose of these scrubbing systems is to remove acidic contaminants from the raw gas stream. As energy sources are being depleted and environmental restrictions are tightening, the economic use of the “bottom of the barrel” in gasification processes is increasing. There are many new projects being sanctioned, most of which would need acid gas clean-up to remove contaminants during processing. Removing CO₂ from flue gases is also important for a variety of reasons, such as a secondary CO₂ market, enhanced oil recovery, and greenhouse gas reduction.

Weak organic bases, such as monoethanolamine (MEA), diethanolamine (DEA), and methyldiethanolamine (MDEA) comprise many of the typical alkanolamine solvents known in the art. MDEA is known to have advantages for CO₂ removal and other acid gas contaminants in high-pressure gas streams. The amount of energy required to regenerate the MDEA is low because it is a relatively weak base and therefore the chemical bond formed during the reaction with CO₂ is weaker than with other commonly used alkanolamines. A secondary benefit lies in the nature of the chemical bond formed during absorption. As a tertiary alkanolamine, MDEA reacts with CO₂ to form a bicarbonate ion rather than a carbamate, which results in a reaction ratio MDEA to CO₂ of 1:1. In contrast, other commonly used primary and secondary alkanolamines preferentially form a carbamate and require a reaction ratio of 2:1. The reaction between CO₂ and tertiary alkanolamines (e.g., MDEA) is typically of a greater efficiency than between CO₂ and other commonly used primary and secondary alkanolamines. These combined benefits result in a process of greater efficiency and capacity than is possible with commercial primary and secondary alkanolamines such as MEA and DEA.

A disadvantage of using tertiary alkanolamines is that CO₂ is indirectly absorbed, resulting in a weak driving force and slow rate of reaction compared to other commercial alkanolamines. In high-pressure gas contacting systems the effect of the weak driving force is minimized due to the higher fraction of CO₂ that can be achieved in the liquid resulting from the high CO₂ partial pressure in the gas above it. When gasses are contacted at low pressure, the driving force is weak as the partial pressure of CO₂ is also weak. Thus, there is no beneficial effect of pressure, and the CO₂ equilibrium established between the gas and liquid is low. Tertiary alkanolamines are not normally used in low-pressure applications because of their low equilibrium loading. Other more commonly used primary and secondary amines such as MEA and DEA, which are stronger bases, are used in these applications due to their higher driving force and increased rate of reaction with CO₂. In these low-pressure situations, the disadvantage of the inefficient carbamate reaction is outweighed by the greater equilibrium liquid distribution achieved.

In an effort to increase the capacity of MDEA for CO₂ at low partial pressure, a number of improvements to the basic MDEA process have been developed. These improvements typically involve the addition of small amounts of primary or secondary amines to the MDEA solution (as described in U.S. Pat. Nos. 5,209,914 and 5,366,709 and PCT Application No. WO 03/013699). The resulting mixtures are commonly described as formulated or blended MDEA with additives referred to as “catalysts,” “absorption accelerators,” or “activators” (e.g., U.S. Pat. No. 6,740,230). These additives generally function by increasing the rate of CO₂ absorption into the MDEA blend solution at low CO₂ partial pressure thereby increasing the fraction of CO₂ in the liquid as compared to the MDEA solution alone.

Although effective in the removal of CO₂ as described, the commercial application of known formulated solvents has less than ideal operating characteristics. Some of the additives used for formulating have limited solubility in MDEA, which reduces their effectiveness, and their commonly lower boiling points (some are not lower) in turn create difficulties in maintaining their concentration. Moreover, the reaction products of the additives with CO₂ are also problematic. As they are stronger organic bases than MDEA these blends have a tendency to require more energy for regeneration and their products have limited solubility. Such characteristics limit their effectiveness and the efficiency of the overall process if their concentration exceeds approximately 20% of the total amine in solution.

There thus exists an industrial need for improved compositions and methods for recovering acidic contaminants from both high and low pressure systems. A particular need exists for products having the benefits of both low-pressure equilibrium capacity of primary or secondary amines and the efficiency of tertiary amines within a single compound of reduced volatility.

BRIEF SUMMARY OF THE INVENTION

This invention accordingly provides novel compositions for removing carbon dioxide and acidic sulfide contaminants from fluid streams, for example, natural gas, synthesis gas, combustion gas, biogas, and other industrial fluid streams. Through this disclosure reference to gas or fluid streams is intended to encompass, without limitation, all such fluids. In a preferred embodiment, the compositions of the invention are used for removal, absorption, or sequestration of CO₂. In other preferred embodiments, the compositions are used for removal of other acidic contaminants, including, without limitation, acidic and sulfide contaminants, such as CO₂, H₂S, RSH, CS₂, COS, and SO₂.

In an aspect, the invention is an absorbent liquid composition for absorbing acidic contaminants from fluid streams in an industrial process. The composition includes at least one absorbent component having the following general formula, structure (I).

R₁ is H, alkyl, aminoalkyl, or structure (II). Preferably, if R₁ is H, then at least one of R₁₀, R₁₁, R₁₂, or R₁₃ is not H, and if R₁ is structure (II), then at least one of R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, R₁₆, or R₁₇ is not H. Each R₂, R₃, R₄, R₅, R₆, R₇, R₈, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, R₁₆, and R₁₇ are independently H, alkyl, or aminoalkyl, and each m, n, and o are independently 0, 1, or 2 and each p and q are independently 0, 1, 2, 3, or 4.

In another aspect, the invention is a process for reducing acidic contaminants in an industrial fluid stream. The process includes contacting the fluid stream with the described composition to form a washed fluid stream and a rich acid gas scrubbing liquid. At least a portion of the composition including at least a portion of the described absorbent component(s) is regenerated from the rich acid gas scrubbing liquid.

It is an advantage of the invention to provide a novel composition having a specific molecular structure that offers reduced volatility and a working capacity for acidic contaminants greater than commonly used alkanolamine solvents in both low and high-pressure environments.

It is another advantage of the invention to provide a novel composition that reduces acidic contaminants in natural, synthesis, and flue gases and has an increased liquid capacity for acidic contaminants at low gas pressure.

An additional advantage of the invention is to provide a novel composition that reduces acidic contaminants in natural, synthesis, and flue gases and has reduced energy of regeneration.

Another advantage of the invention is to provide a novel composition that reduces acidic contaminants in natural, synthesis, and flue gases and has increased depth of removal.

It is a further advantage of the invention to provide a novel composition that reduces acidic contaminants in natural, synthesis, and flue gases and has improved stability in the process compared to current solvents.

It is an additional advantage of the invention to provide a novel composition that reduces acidic contaminants in natural, synthesis, and flue gases and has improved viscosity and regenerability in the process compared to current solvents.

It is yet another advantage of the invention to provide a novel composition that reduces acidic contaminants in natural, synthesis, and flue gases and has a higher boiling point resulting in minimized losses from the process and reduced corrosivity.

The foregoing has outlined rather broadly the features and technical advantages of the present invention in order that the detailed description of the invention that follows may be better understood. Additional features and advantages of the invention will be described hereinafter that form the subject of the claims of the invention. It should be appreciated by those skilled in the art that the conception and the specific embodiments disclosed may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. It should also be realized by those skilled in the art that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a simplified process diagram demonstrating the configuration of the equipment in a typical amine solvent wash system.

DETAILED DESCRIPTION OF THE INVENTION

The following definitions are intended to be clarifying and are not intended to be limiting.

“Alkyl” refers to a monovalent group derived from a straight or branched chain saturated hydrocarbon by the removal of a single hydrogen atom. Representative alkyl groups include methyl; ethyl; n- and iso-propyl; n-, sec-, iso-, and tert-butyl; C₅ to C₁₂ groups; eicosanyl (C₂₀); heneicosanyl (C₂₁); docosyl (behenyl, C₂₂); tricosanyl (C₂₃); tetracosanyl (C₂₄); pentacosyl (C₂₅), 3-, 7-, and 13-methylhexadecanyl; and the like. Preferred alkyls include methyl, ethyl, propyl, isopropyl, butyl, and isobutyl.

“Aliphatic amine” and/or “aminoalkyl” refers to an alkyl group having one or more amino substitutions or an amino group having multiple alkyl substitutions. Representative aminoalkyls include aminomethyl, dimethylaminomethyl, diethylaminomethyl, 2-aminoethyl, 2-dimethylaminoethyl, 2-ethylaminoethyl, and the like.

“Amino” or “amine” refers to a group having the structure —NR′R″, wherein R′ and R″ are independently selected from H and alkyl, as previously defined. Additionally, R′ and R″ taken together may optionally be —(CH₂)_(k)— where k is an integer of from 2 to 6. Representative amino groups include, amino (—NH₂), methylamino, ethylamino, n- and iso-propylamino, dimethylamino, methylethylamino, piperidino, and the like.

“Depth of removal” refers to the amount of CO₂ that escapes the absorbent solution during peak performance (i.e., CO₂ slip), and is an approximation of the efficiency of CO₂ absorption.

“Heterocyclic amine” refers to a substituted carbocyclic structure containing at least one nitrogen member in the ring.

“Working capacity” refers to the difference between rich loading and lean loading.

This invention has application in a wide array of industrial processes including gas fields (e.g., marginal, stranded, and sour gas fields), liquefied natural gas (LNG) liquefaction developments, gas-to-liquids (GTL) developments, synthesis gas, and for the removal of CO₂ from combustion gases. The disclosed composition may be used in any industrial process, such as single or multi-injection, known in the art or in any specialized high-pressure processes, such as those described in U.S. Pat. No. 6,497,852, “Carbon Dioxide Recovery at High Pressure” and U.S. Pat. No. 7,481,988, “Method for Obtaining a High Pressure Acid Gas Stream by Removal of the Acid Gases from a Fluid Stream,” and in PCT patent application no. WO2007077323A1, “Method for Deacidifying a Gas with a Fractionally-Regenerated Absorbent Solution with Control of the Water Content of the Solution.”

Referring to FIG. 1, an exemplary production process (typically found in natural gas processing) where this invention has utility is shown. Production process 100 includes raw gas inlet 105 where gas is contacted counter currently (typically at pressures greater than atmospheric) with a lean solvent solution (i.e., containing very low concentrations of acidic contaminants) in absorber column 110. The rich solvent solution (i.e., containing high concentrations of acidic contaminant(s) absorbed from the feed gas) drains out of absorber column 110 and passes via a pressure reduction valve (not shown) to rich amine flash drum 115 where co-absorbed volatile hydrocarbons and a portion of the absorbed acid gas contaminate is flashed from the solvent and removed into a vapor discharge stream from the drum.

Treated gas outlet 120 contains gas exiting the top of absorber column 110, treated and freed of acid gas contaminant(s). The rich amine solvent exits rich amine flash drum 115 and proceeds through rich/lean amine exchanger 125, where it is heated, and then into the top of regenerator column 130, where the acid gas contaminant(s) is separated from the rich solution at low pressure and high temperature as the solvent flows down the column. The rich solvent is stripped in the column by a countercurrent steam flow produced in amine reboiler 135 at the base of the column. The hot regenerated solvent accumulates at the base of the column and the stripped contaminant(s) gasses exit the top of the column with the stripping steam.

Steam and solvent vapor exiting the top of regenerator column 130 enters acid gas condenser 140. Resulting liquids are collected in reflux drum 145 for circulation back to the top of the regenerator column through reflux circulation pump 165. The regenerated hot lean solvent is pumped from the base of regenerator column 130 via rich/lean exchanger 125 (through lean amine circulation pump 160) and lean amine cooler 150 back into the top of absorber column 110 (through lean amine pressure pump 170), where the cycle is repeated. Filtration of lean solvent at lean amine filter 155 keeps it clear of solids and contaminants including degradation products caused by adverse components of the raw feed gas stream. It should be appreciated that filtration could take place in multiple and various locations in the process.

In one embodiment, the composition of this invention includes at least one substituted cyclic diamine component (as shown in structure (I) above). In a preferred embodiment, the composition of this invention includes substituted piperazine moieties with substitution at the 1 and/or 4 nitrogen positions of the piperazine ring as well as substitution at the 2, 3, 5, and/or 6 positions. In other embodiments, the composition includes substituted cyclic diamines having a 4- to 12-membered ring.

Exemplary structures of typical N-mono- or N-bi-substituted piperazines of the invention are shown as structure (III) below, where R₁₈ is H, alkyl, aminoalkyl, or structure (IV); R is structure (II) shown below, and R₁₉, R₂₀, R₂₁, R₂₂, R₂₃, R₂₄, R₂₅, and R₂₆ are independently H, alkyl, or aminoalkyl.

R₂₇, R₂₈, R₂₉, R₃₀, R₁₄, R₁₅, R₁₆, and R₁₇ are independently H, alkyl, or aminoalkyl, and each m, n, o, x, y and z is independently 0, 1, or 2. In a preferred embodiment, if R₁₈ is H at least one of R₁₄, R₁₅, R₁₆, or R₁₇ is not H, and if R₁₈ is structure (II) at least one of R₂₇, R₂₈, R₂₉, R₃₀, R₁₄, R₁₅, R₁₆, or R₁₇ is not H.

In a further embodiment, the composition of the invention includes N-mono- and N-bisubstituted aminopiperazines, which may be substituted in the 2, 3, 5, and/or 6 positions of the piperazine ring. The substitutions are typically methyl, ethyl, propyl, isopropyl, or dimethyl. It should be appreciated that although the 2, 3, 5, and 6 unsubstituted piperazines are proficient CO₂ absorbents, significant advantages exist in utilizing the 2, 3, 5, and 6 substituted variants. Particularly reductions in process viscosity and improved regenerability are observed.

Structure (V) below illustrates a representative structure for the bisubstituted piperazine embodiment of the invention. R₃₁, R₃₂, R₃₃, R₃₄, R₃₅, R₃₆, R₃₇, R₃₈, R₃₉, R₄₀, R₄₁, R₄₂, R₄₃, R₄₄, R₄₅ and R₄₆ are independently H, alkyl, or aminoalkyl. Preferred alkyls include methyl, ethyl, propyl, isopropyl, butyl, and isobutyl. Preferred aminoalkyls include 2-aminopropyl, 2-aminobutyl, aminoethyl, and aminopropyl. In a preferred embodiment, at least one of R₃₁, R₃₂, R₃₃, R₃₄, R₃₅, R₃₆, R₃₇, or R₃₈ is not H and at least one of R₃₉, R₄₀, R₄₁, R₄₂, R₄₃, R₄₄, R₄₅, or R₄₆ is not H. The value of each s, t, and u are independently 0, 1, or 2.

Representative monosubstituted piperazines include 2-aminopropyl-piperazine, 2-aminobutyl-piperazine, 1-acetylpiperazine, and 1-formylpiperazine. Representative examples of typical bisubstituted piperazines include 1,4-bis-(2-aminopropyl)-piperazine; 1,4-bis-(2-aminobutyl)-piperazine; 1,4-bis-(3-aminobutyl)-piperazone; 1,4-bis-(N-methyl-aminoethyl)-piperazine; 1-(2-aminobutyl)-4-methylpiperazine; 1-(2-aminopropyl)-4-methylpiperazine; and 1-(2-aminopropyl)-4-ethylpiperazine; 1-aminoethyl-4-(2-aminobutyl)-piperazine; 1-aminoethyl-4-(2-aminopropyl)-piperazine; 1-aminopropyl-4-(3-aminobutyl)-piperazine; 1-aminoethyl-4-(N-methyl-aminoethyl)-piperazine; the like; and combinations thereof.

In one embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (1-14) where R═H, or more preferably R is selected from methyl, ethyl, propyl, isopropyl, and combinations thereof.

In another embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (15-21).

In an additional embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (22-35).

In yet another embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (36-42).

In another embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (43-49), where R═H, or more preferably R is selected from methyl, ethyl, propyl, isopropyl, and combinations thereof.

In another embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (50-56).

In a further embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (57-63).

In one embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (64-77).

In a further embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (78-84).

In another embodiment, the composition of the invention includes at least one n absorbent component of the formulas illustrated in structures (85-91).

In another embodiment, the composition of the invention includes at least one absorbent component of the formulas illustrated in structures (91-97).

The composition of the invention may also include derivatives and/or salts of the disclosed structures. Representative derivatives include carbonates, bicarbonates, carbamates, ureas, and amides. Representative salts include all inorganic, mineral, and organic salts.

It is the intent of this invention to use the disclosed structures in a multitude of compositions including single or multiple component solutions in water or as combined with other acid gas solvent components such as tetramethylene sulfone (i.e., Sulfolane), MDEA, DEA, MEA, and the like in water and/or other mutual solvents.

For example, single and multiple component solutions range from about 0.01 to about 100 wt % actives or from about 1 to about 75 wt % actives and include the use of solvents, such as water, alcohols, polyols, other acid gas solvents, and organic solvents. In a preferred embodiment, the composition includes about 10 to about 75 wt % or from about 40 to about 50 wt % actives. Additionally, the composition generally includes an amount of solvent in the range of 0 to 99.09 wt %, depending upon the amount of actives.

The scrubbing liquid used in the composition of the invention may also include, for example, one or more of the following components: aminoethyl-piperazine; 2-aminoethyl-piperazine; 2-aminopropyl-piperazine; 2-aminobutyl-piperazine; 1-acetylpiperazine; 1-formylpiperazine; 1,4-bis-aminoethyl-piperazine; 1,4-bis-aminopropyl-piperazine; 1,4-bisaminobutyl-piperazine; 1,4-bis-(2-aminopropyl)-piperazine; 1,4-bis-(2-aminobutyl)-piperazine; 1,4-bis-(N-methyl-aminoethyl)-piperazine; 1-(2-aminobutyl)-4-methylpiperazine; 1-(2-aminopropyl)-4-methylpiperazine; 1-(2-aminopropyl)-4-ethylpiperazine; 1-aminoethyl-4-(2-aminobutyl)-piperazine; 1-aminoethyl-4-(2-aminopropyl)-piperazine; 1-aminoethyl-4-(N-methyl-aminoethyl)-piperazine; 2-morpholinoethanamine; 2-aminopropyl-morpholine; 2-(1H-imidazol-1-yl)ethanamine; 2-aminopropyl-piperidine; 2-aminopropyl-pyrrolidine; N1-(2-aminopropyl)butane-1,4-diamine; N1-(3-aminopropyl)propane-1,2-diamine; water; sulfolane, N-methylpyrrolidone; N-alkylated pyrrolidones, piperidones and morpholines corresponding to the foregoing; methanol; mixtures of dialkyl ethers of polyethylene glycols; C₁ to C₄ dialkylether monoethylene glycols; C₁ to C₄ monoether monoethylene glycols; C₁ to C₄ dialkylether poly ethylene glycols; C₁ to C₄ monoether polyethylene ethylene glycols; C₁ to C₄; ethylene glycol; diethylene glycol; triethylene glycol; N,N-dimethyl formamide; N-acetyl morpholine; N-formyl morpholine; N,N-dimethyl imidazolidin-2-one; N-methyl imidazole; and the like.

In another embodiment, the composition of the invention may also include other components. Representative other components include blends of amines, activators, promoters, antifoaming agents, co-absorbents, corrosion inhibitors, solvents, coloring agents, the like, and combinations thereof. Representative examples include alkanolamines; cyclotetramethylene sulfone and its derivatives; aliphatic acid amines such as acetyl morpholine or N-formyl morpholine; alkali metal compounds which provide alkaline hydrolysis products, such as alkali metal hydrolysis and hydrocarbonates; aliphatic and cycloaliphatic mono- and diamines, such as triethylene diamine, dicyclohexyl amine, N-ethyl-cyclohexylamine, and N,N-diemthylcyclohexylamine; the like; and combinations thereof.

In various embodiments, the absorbent of the invention may include coabsorbents as disclosed in, for example, U.S. patent application Ser. No. 12/494,521, “Acid Gas Scrubbing Composition,” filed Jun. 30, 2009 and currently pending, Ser. No. 12/494,533, “Acid Gas Scrubbing Composition,” filed Jun. 30, 2009 and currently pending, and U.S. Pat. No. 8,318,114, “Composition for Treating Acid Gas,” filed Apr. 6, 2010.

In another embodiment, coabsorbents include one or more components selected from calcium oxide, calcium lignosulfonate, calcium silicate hydrates, calcium hydroxide, calcium carbonate, calcium bicarbonate, sodium carbonate, sodium bicarbonate, trona, sodium sesquicarbonate, soda ash, nacholite, sodium aluminate, metal oxides, and the like.

Activators and coabsorbents are preferably present in the composition of the invention from about 0.01 to about 90 wt %, more preferably from about 1 to about 50 wt %, and most preferably from about 1 to about 25 wt % (wt % based on the weight of total actives).

In a further embodiment, the invention is a process for reducing acidic contaminants in an industrial fluid stream. The fluid stream is contacted with the disclosed composition to form a washed fluid stream and a rich acid gas scrubbing liquid. Typically, the composition is contacted with the gas stream at a temperature ranging from about 0 to about 200° C. In certain cases, this temperature range may be from about 0 to about 100° C. or from about 20 to about 65° C. Industrial processes generally run at a pressure ranging from about 0 to about 200 atm, from about 0 to about 100 atm, from about 0 to about 70 atm, from about 0 to about 50 atm, from about 0 to about 25 atm, from about 0 to about 10 atm, or from about 1 to about 5 atm during the time when the composition is contacted with the fluid stream. U.S. Pat. No. 4,556, “Bis Tertiary Amino Alkyl Derivatives as Solvents for Acid Gas Removal from Gas Streams” discloses pressure ranges from 4 to 70 atm. Canadian patent application no. 2,651,888, “Carbon Dioxide Absorbent Requiring Less Regeneration Energy” discloses pressures from 1 to 120 atm. It should be appreciated that this invention is operable in any of these or other pressure ranges encountered in the relevant art.

The rich acid gas scrubbing liquid is further processed through a regeneration system where at least a portion of the composition including at least a portion of the absorbent compound(s) contacted with the fluid stream are regenerated. The regeneration step normally takes place at a higher temperature than absorption (depending on the particular industrial process), usually at a temperature ranging from about 0 to about 500° C., from about 20 to about 250° C., or from about 50 to about 150° C. The pressure range for the regeneration step is normally from about 0 to about 10 atm or from about 1 to about 5 atm. In certain cases, the regeneration step may be carried out via a steam-assisted reboiler. Regeneration may also be carried out via a fractional regeneration process (e.g., WO 2007/077323, “Method for Deacidifying a Gas with a Fractionally-Regenerated Absorbent Solution with Control of the Water Content of the Solution”).

The foregoing may be better understood by reference to the following examples, which are intended for illustrative purposes and are not intended to limit the scope of the invention.

Example 1

The testing in this Example was used as a means of screening potential acidic contaminant scavengers and also to confirm the performance of existing commercially available scavengers. The test was designed to determine the maximum capacity of an amine solvent in absorbing acidic gases. Different amine solvents were compared. The amine solvents were saturated with acidic gases at a constant pressure and temperature until no more gas was able to be absorbed. The difference between the rich and lean loadings was used to determine the working capacity. The test was designed to regenerate the solvent by boiling to remove the acidic gases so that the lean loading of CO₂ in an amine solvent could be determined.

Solvent performance was characterized by liquid loading at equilibrium with defined composition gas mixtures at simulated amine contactor and regenerator conditions relative to industry benchmarks.

To highlight the advantages of the disclosed novel amines, several specific samples were benchmarked against common commercial CO₂ absorbents (such as 33.8/6.2 wt. %) methyldiethanolamine/piperazine (DMDEA, a derivative of MDEA), monoethanolamine (MEA), and illustrated below) using a laboratory-scale fixed bed absorption cell and a batch reboiler. The “Sorbent” numbers indicated in Table 1 correspond to the structure numbers above and those indicated in below. The equilibrium saturation test to determine the rich loading (weight % CO2 absorbed by fresh sorbent) was run by exposing an aqueous solution of the absorbent at 40° C. to 30 psig of CO₂ until saturation was reached. The lean loading (weight % CO₂ remaining associated with the absorbent after regeneration) was determined by refluxing the aqueous solution of the absorbents for two hours at atmospheric pressure. The working capacity is defined as the rich loading minus the lean loading. It is the working capacity that most accurately reflects the capacity of the chemical to absorb CO₂ under process conditions. The results of this evaluation are reported in Table 1.

To determine rich loading, the equipment consisted of a high pressure gas panel that was capable of receiving supplies of 100% CO₂, CO₂/N₂ mixtures and CO₂/H₂S/N₂ mixtures. The chosen gas was fed via a mass flow controller (Sierra series 100 mass flow controller, available from Sierra Instruments, Inc. in Monterey, Calif.) to the reaction vessel. A gas totalizer (a Sierra Compod) attached to the mass flow controller measured the volume of gas used.

Once the appropriate gas cylinder valve and regulators were opened, the recirculating bath was set to a temperature of 40° C. A 200 ml glass reaction vessel was attached to the head of a Buchi Picoclave. The inlet and outlet valves to the reaction vessel were closed and the inlet pressure regulator was set to 30 psig. The gas mixture was set to 100% CO₂ and the flow rate was set to 0.5 liters/min. After allowing the gas pressure to build to 30 psig at the reactor inlet, the amine solution was prepared at the concentration indicated in Table 1 and, after being brought to the same temperature as the reaction vessel, was added to the reaction vessel and stirred at 1,000 rpm.

The inlet valve was opened and the reactor pressure was allowed to equilibrate to 30 psig. When the pressure in the reactor reached 30 psig, the inlet valve was closed and the gas flow was shut off. The volume in the reactor vessel was recorded. Gas flow was resumed after 5 minutes and continued until the pressure equalized to 30 psig. This procedure was repeated until no additional CO₂ was absorbed as measured by the final volume. The wt % rich loading of the amine was calculated from the final volume of CO₂ absorbed.

To determine lean loading, the amine composition to be regenerated was poured into a 250 ml 3-neck flask equipped with mechanical stirring and a chilled condenser (8° C.). The amine solution was slowly heated to reflux (about 100 to 104° C.) to help avoid a sudden release of gas which would have caused the solution to foam. The solution was refluxed for 2 hours and then cooled to room temperature. The lean loading of the amine was determined via a standard barium chloride back titration.

To determine depth of removal, a mass flow controller (Sierra series 100 mass flow controller) was used to control the flow of gas through the reactor vessel. The chosen gas was fed via the mass flow controller to the saturation vessel (which contained deionized water) and then into the reaction vessel. From the reaction vessel, the gas was fed via a backpressure regulator through a Dreschel bottle containing ethylene glycol and a drying tube containing silica gel to the CO₂ analyzer. The CO₂ analyzer (Signal 7000FM CO₂ analyzer) recorded the concentration of CO₂ flowing through it. The recirculating bath was set to the required temperature of 40° C. The 200 ml glass reaction vessel was fitted to the head of a Buchi Picoclave. A Dreschel bottle containing ethylene glycol and a drying tube containing silica gel was connected to the gas line prior to the CO₂ analyzer, and the backpressure regulator was set to 90 psig. The gas mixture (25% CO₂/75% N₂) and the flow rate (0.45 liters/min) were then set and allowed to stabilize for 30 minutes. The amine solution was prepared at the concentrations indicated in Table 1 and heated as above. The amine was then added to the reaction vessel and the stirrer was set to 1,000 rpm. The downstream regulator was closed and the data recording began. The gas flow was allowed to continue until equilibrium was reached ˜3 hrs. At the end of the run, the gas flow was stopped, the inlet valve to the reaction vessel was closed, and the data recording was stopped.

TABLE 1 NPX Amines vs. Common Absorbents Rich Rich Lean Lean Working Working Depth of Sorbent MW Wt. % (Aq) Loading Mole Ratio Loading Mole Ratio Capacity Mole Ratio Removal 1 (R = methyl) 157.26 40.0% 13.84% 1.44 0.18% <0.01 13.66% 1.41 0.19% 97 157.26 40.0% 12.74% 1.30 0.04% <0.01 12.70% 1.30 0.18% AEP 129.20 40.0% 13.79 1.17 1.02% 0.02 12.77% 1.07 0.10 DMDEA 114.41 40.0% 11.27% 0.83 0.03% <0.01 11.24% 0.82 0.35% MEA 61.08 35.0% 13.50% 0.62 1.41% 0.06 12.09% 0.55 0.00%

The tested amines on average absorbed about 1.36 moles of CO₂ per mole of absorbent compared to less than 0.83 mole of CO₂ per mole of the common absorbents. Although 97 only slightly outperformed the common absorbents sorbent 1 (R=methyl) showed a significant increase in working capacity (13% increase based on MEA; 22% increase based on DMDEA). These novel amines also have a significantly lower lean loading than MEA.

The boiling points of the disclosed amines range from about 200 to about 280° C. at 1 atm (compared to MEA at 170° C. and 1 atm). Such higher boiling points help significantly reduce the losses and potential environmental releases currently associated with the volatility of MEA and also help to prevent CO₂ contamination during solvent regeneration. Initial laboratory stability testing has indicated that unlike MEA, which is known to degrade rapidly under process condition, the disclosed amines are highly robust at simulated process conditions showing no signs of degradation.

To further highlight the utility of the tested amines for carbon capture, a 25% CO₂ gas stream at 90 psig was passed through the absorbents at 40° C. until they reached saturation and the depth of removal was recorded. Importantly, the depth of removal for many of the tested amines approached 0%, an indication that they are highly efficient at CO₂ capture as shown in Table 1.

Example 2

Although a reduction in the lean loading of branched compounds over linear compounds would have been expected, the select group of molecules tested also showed a unique increase in the rich mole ratio of the branched targets (Table 1)). This unusual reactivity is particularly evident when comparing the linear AEP, a promoter known in the industry, to the branched sorbents 97 and 1 (R=methyl). This increase in molar capacity is thought to occur via a change in the mechanism by which the amine reacts with CO₂. Thus, the reactions between CO₂ and the branched amines are of greater efficiency.

Example 3

This Example compared the absorption Sorbents 97 and 1 (R=methyl). The two molecules are identical in molecular weight and were tested under identical conditions; however, Sorbent 1 (R=methyl) shows a 7.6% increase in working capacity, and significantly improved in process viscosity and improved process regenerability. This effect has been attributed to the substitution of the piperazine ring carbon.

The rate of transfer of a solute between a gas and a liquid is proportional to the liquid film area which is the contact surface between the two phases. This contact area will be beneficially greater in a liquid which has a lower viscosity as compared against a benchmark liquid of greater viscosity due to the decrease in mean gas bubble diameter in the lower viscosity liquid and resulting increase in contact surface area as compared against the liquid of greater viscosity.

This benefit is realized in both absorption and desorption of the solute into and out of a liquid phase. In an absorption column the increase in surface contact area proportionally increases the volumetric mass transfer coefficient k₁a therefore reducing the amount of contact time required to achieve a required solute transfer fraction from gas to liquid phase. In a desorption column, the increase in surface area again benefits the mass transfer, but this time out of the liquid phase and into the stripping gas phase resulting in a reduction in contact time required to achieve the required reduction in liquid phase concentration of the solute as compared to the more viscous benchmark.

All of the compositions and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While this invention may be embodied in many different forms, there are described in detail herein specific preferred embodiments of the invention. The present disclosure is an exemplification of the principles of the invention and is not intended to limit the invention to the particular embodiments illustrated. In addition, unless expressly stated to the contrary, use of the term “a” is intended to include “at least one” or “one or more.” For example, “a device” is intended to include “at least one device” or “one or more devices.”

Any ranges given either in absolute terms or in approximate terms are intended to encompass both, and any definitions used herein are intended to be clarifying and not limiting. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. Moreover, all ranges disclosed herein are to be understood to encompass any and all subranges (including all fractional and whole values) subsumed therein.

Furthermore, the invention encompasses any and all possible combinations of some or all of the various embodiments described herein. Any and all patents, patent applications, scientific papers, and other references cited in this application, as well as any references cited therein, are hereby incorporated by reference in their entirety. It should also be understood that various changes and modifications to the presently preferred embodiments described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the invention and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered by the appended claims. 

The claimed invention is:
 1. A scrubbing liquid composition for absorbing acidic contaminants from fluids in an industrial process, the composition comprising at least one absorbent component, wherein said absorbent component includes at least one selected from the group consisting of: structures 1-9, 11-14 and 43-49, wherein R=methyl, ethyl, propyl, isopropyl, and combinations thereof


2. The composition of claim 1, wherein said absorbent component further includes at least one selected from the group consisting of: structures 15-21 and 50-56, and combinations thereof


3. The composition of claim 1, wherein said absorbent component further includes at least one selected from the group consisting of: structures 22-35 and 57-63, and combinations thereof


4. The composition of claim 1, wherein said absorbent component further includes at least one selected from the group consisting of: structures 64-84, and combinations thereof


5. The composition of claim 1, wherein said absorbent component further includes at least one selected from the group consisting of: structures 36-42 and 85-91, and combinations thereof


6. The composition of claim 1, wherein said absorbent component further includes at least one selected from the group consisting of: structures 92-97 and combinations thereof


7. The composition of claim 1, wherein the absorbent component further includes at least one selected from the group consisting of: 2-aminopropyl-piperazine; 2-aminobutyl-piperazine; 1-acetylpiperazine; 1-formylpiperazine; 1,4-bis-aminoethyl-piperazine; 1,4-bis-aminopropyl-piperazine; 1,4-bisaminobutyl-piperazine; 1,4-bis-(2-aminopropyl)-piperazine; 1,4-bis-(2-aminobutyl)-piperazine; 1,4-bis-(N-methyl-aminoethyl)-piperazine; 1-(2-aminobutyl)-4-methylpiperazine; 1-(2-aminopropyl)-4-methylpiperazine; 1-(2-aminopropyl)-4-ethylpiperazine; 1-aminoethyl-4-(2-aminobutyl)-piperazine; 1-aminoethyl-4-(2-aminopropyl)-piperazine; 1-aminoethyl-4-(N-methyl-aminoethyl)-piperazine; 2-morpholinoethanamine; 2-aminopropyl-morpholine; 2-(1H-imidazol-1-yl)ethanamine; 2-aminopropyl-piperidine; 2-aminopropyl-pyrolidine; N1-(2-aminopropyl)butane-1,4-diamine; N1-(3-aminopropyl)propane-1,2-diamine; water; sulfolane, N-methylpyrrolidone; N-alkylated pyrrolidones, piperidones and morpholines corresponding to the foregoing; methanol; mixtures of dialkyl ethers of polyethylene glycols; C₁ to C₄ dialkylether monoethylene glycols; C₁ to C₄ monoether monoethylene glycols; C₁ to C₄ dialkylether poly ethylene glycols; C₁ to C₄ monoether polyethylene ethylene glycols; C₁ to C₄; ethylene glycol; diethylene glycol; triethylene glycol; N,N-dimethyl formamide; N-acetyl morpholine; N-formyl morpholine; N,N-dimethyl imidazolidin-2-one; N-methyl imidazole; and combinations thereof.
 8. The composition of claim 1, wherein the acidic contaminant is selected from the group consisting of: CO₂, H₂S, RSH, CS₂, COS, SO₂, and combinations thereof.
 9. The composition of claim 1, wherein said absorbent compound is present in an amount ranging from about 0.01 to about 100 wt %.
 10. The composition of claim 1, further comprising at least one component selected from the group consisting of: amines, activators, promoters, antifoaming agents, co-absorbents, corrosion inhibitors, coloring agents, and combinations thereof.
 11. The composition of claim 1 further comprising a solvent, wherein the solvent is selected from the group consisting of: water, alcohols, polyols, other acid gas solvents, organic solvents, and combinations thereof. 